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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431350Generated: November 2, 2026

3-Methoxypropylamine → HCID 59631510, compound

https://huagongshe.com/reaction/1431350

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxypropylamineHCID 1672—
Reactant5-Bromo-2-chloro-3-nitropyridineHCID 7019412—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 59631510HCID 59631510—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a 100 mL round bottom flask containing 5-bromo-2-chloro-3-nitropyridine (5.12 g, 21.6 mmol) in DMSO (20.5 mL) was added 3-methoxypropylamine (4.40 mL, 43.1 mmol) dropwise. The reaction was heated to 60° C. and monitored with TLC and LC-MS. After 2.5 h, LC-MS showed that the reaction was complete. The mixture was cooled to rt then diluted with water. After extracting three times with EtOAc, the organic layers were combined then washed with brine and dried over anhydrous magnesium sulfate. After filtration, the mixture was concentrated in vacuo to give a light yellow brown solid as 5-bromo-N-(3-methoxypropyl)-3-nitropyridin-2-amine. 1H NMR (400 MHz, CDCl3) δ ppm 8.62 (1H, br. s.), 8.54 (1H, d, J=2.3 Hz), 8.43 (1H, d, J=2.3 Hz), 3.69-3.78 (2H, m), 3.56 (2H, t, J=5.7 Hz), 3.40 (3H, s), 1.96 (2H, dt, J=12.2, 6.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940724B2
Source datasetuspto-grants-2015_01
ORD IDord-8eff9fcbaee941aeadae29091a0be71b
Source noteuspto-grants-2015_01